Establishment of Quantitative SPR Assay for Antibodies Against Human Platelet Antigen-1a.
10.19746/j.cnki.issn.1009-2137.2021.01.039
- Author:
Rui-Shu LI
1
;
Ming-Chen NI
2
;
Hui-Jun ZHU
1
;
Qin-Qin MA
1
;
Min FU
1
;
Ping LU
3
Author Information
1. Shanghai Blood Center, Shanghai Institute of Blood Transfusion, Shanghai 200051, China.
2. Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
3. Shanghai Blood Center, Shanghai Institute of Blood Transfusion, Shanghai 200051, China,E-mail: luping@sbc.org.cn.
- Publication Type:Journal Article
- MeSH:
Antigens, Human Platelet;
Blood Platelets;
Humans;
Isoantibodies;
Surface Plasmon Resonance
- From:
Journal of Experimental Hematology
2021;29(1):239-242
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To establish quantitative surface plasmon resonance (SPR) assay for antibodies against human platelet antigen-1a (HPA-1a).
METHODS:Recombinant protein was fixed on the chip surface by amino coupling method. SPR assay was used to detect the standard antibodies against HPA-1a at different conceatration. The optimal experimental parameters were determined, and standard curves were constructed with linear regression. Moreover, the sensitivity, specificity, accuracy and precision of the assay were evaluated.
RESULTS:The quantitative SPR assay for HPA-1a antibodies was established. The determination ranges were 0-20 IU, with accuracy (recovery rate) was 97.75%-103.08%. The intra-assay precision [coefficients of variation (CV)] was 3.53%-4.29%, and the inter-assay precision (CV) was 2.08%-4.40%. For specificity test, several kinds of monoclonal and human antibodies against platelet membrane protein were tested and no positive result was observed.
CONCLUSION:The established quantitative SPR assay for HPA-1a antibodies shows good sensitivity, specificity, accuracy and precision, and this rapid and simple method provides a new reference method for scientific research and clinical antibody detection.